Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454132Generated: November 2, 2026

Thionyl Chloride → 2-Chloro-3-fluoro-7-methoxyquinoline

https://huagongshe.com/reaction/454132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3-fluoro-7-methoxyquinolin-2(1H)-oneHCID 15260580—
CatalystDimethylformamideHCID 6228—
Product2-Chloro-3-fluoro-7-methoxyquinolineHCID 2203059197%

Reaction Steps

3-Fluoro-7-methoxyquinol-2(1H)-one (300 mg, 1.55 mmol), (prepared as in Tetrahedron, Vol. 52, No. 9, pp. 3223-3228, 1996), was dissolved in thionyl chloride (3 ml), treated with DMF (1 drop) and heated at reflux for 1 hour. The excess thionyl chloride was removed by evaporation and the residue azeotroped with toluene (3×). The residue was basified to pH8 with saturated aqueous sodium hydrogen carbonate solution and extracted with ethyl acetate (3×20 ml). The organic solution was washed with water and brine then dried (MgSO4) and evaporated to dryness to give 2-chloro-3-fluoro-7-methoxyquinoline (320 mg, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492560B2
Source datasetuspto-grants-2013_07
ORD IDord-b0315f4f00794cdf8cf97696b2319539
Source noteuspto-grants-2013_07